Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 844501-71-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized pyrazole integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions. The tetramethyl-dioxaborolane moiety provides exceptional stability and moisture tolerance, enabling reliable use in diverse synthetic workflows.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its pyrazole core provides orthogonal reactivity and enhanced solubility, enabling efficient incorporation into heterocyclic scaffolds. The tetramethyl-substituted dioxaborolane moiety ensures high functional group tolerance and minimal protodeboronation, facilitating reliable coupling with aryl, vinyl, and heteroaryl halides under standard catalytic conditions.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: